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Weekly pulmonary delivery of β-glucan-chitosan-poly(lactic co-glycolic) acid (β-C-P) nanoparticles with daily standard oral therapy achieves control of Mycobacterium tuberculosis in BALB/c mice

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

Abstract

Prolonged daily tuberculosis therapy contributes to toxicity, poor adherence, and drug resistance. We developed rifampin (RIF)-loaded β-glucan-chitosan-poly (lactic co-glycolic) acid nanoparticles (β-C-P nanoparticles) for weekly pulmonary delivery and evaluated a hybrid dosing regimen in a BALB/c Mycobacterium tuberculosis model. Weekly instilled RIF loaded 20% β-C-P nanoparticles combined with daily oral isoniazid (INH) and pyrazinamide (PZA) reduced lung and spleen bacterial burdens comparable to oral daily standard of care (RIF, INH, PZA) and were well tolerated, demonstrating preserved efficacy with reduced RIF dosing frequency.

Original languageEnglish
Article numbere00281-26
JournalAntimicrobial Agents and Chemotherapy
Volume70
Issue number6
DOIs
StatePublished - Jun 2026

Keywords

  • Mycobacterium tuberculosis
  • PLGA
  • isoniazid
  • nanoparticles
  • pyrazinamide
  • rifampin
  • tuberculosis
  • β-glucan

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